Package 72865-206-18
Brand: sertraline hydrochloride
Generic: sertraline hydrochloridePackage Facts
Identity
Package NDC
72865-206-18
Digits Only
7286520618
Product NDC
72865-206
Description
180 TABLET in 1 BOTTLE (72865-206-18)
Marketing
Marketing Status
Brand
sertraline hydrochloride
Generic
sertraline hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "918e3fe6-8b38-4ec8-accb-09b2d82ff404", "openfda": {"upc": ["0372865205303", "0372865205907", "0372865207307", "0372865206904", "0372865205181", "0372865205051", "0372865206188", "0372865207901", "0372865206058", "0372865206300", "0372865207055", "0372865207185"], "unii": ["UTI8907Y6X"], "rxcui": ["312938", "312940", "312941"], "spl_set_id": ["5b73a90e-b883-419b-b30f-a379eed764d9"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-206-05)", "package_ndc": "72865-206-05", "marketing_start_date": "20210503"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (72865-206-18)", "package_ndc": "72865-206-18", "marketing_start_date": "20210503"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72865-206-30)", "package_ndc": "72865-206-30", "marketing_start_date": "20210503"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72865-206-90)", "package_ndc": "72865-206-90", "marketing_start_date": "20210503"}], "brand_name": "SERTRALINE HYDROCHLORIDE", "product_id": "72865-206_918e3fe6-8b38-4ec8-accb-09b2d82ff404", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72865-206", "generic_name": "sertraline hydrochloride", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SERTRALINE HYDROCHLORIDE", "active_ingredients": [{"name": "SERTRALINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA214790", "marketing_category": "ANDA", "marketing_start_date": "20210503", "listing_expiration_date": "20261231"}